Deficiency in Origin Licensing Proteins Impairs Cilia Formation: Implications for the Aetiology of Meier-Gorlin Syndrome
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Title
Deficiency in Origin Licensing Proteins Impairs Cilia Formation: Implications for the Aetiology of Meier-Gorlin Syndrome
Authors
Keywords
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Journal
PLoS Genetics
Volume 9, Issue 3, Pages e1003360
Publisher
Public Library of Science (PLoS)
Online
2013-03-15
DOI
10.1371/journal.pgen.1003360
References
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Related references
Note: Only part of the references are listed.- Human and Mouse Mutations in WDR35 Cause Short-Rib Polydactyly Syndromes Due to Abnormal Ciliogenesis
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- (2011) Louise S Bicknell et al. NATURE GENETICS
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- Human origin recognition complex is essential for HP1 binding to chromatin and heterochromatin organization
- (2010) S. G. Prasanth et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Ciliary biology: Understanding the cellular and genetic basis of human ciliopathies
- (2009) Magdalena Cardenas-Rodriguez et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS
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- Pericentrin, a centrosomal protein related to microcephalic primordial dwarfism, is required for olfactory cilia assembly in mice
- (2009) Ko Miyoshi et al. FASEB JOURNAL
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- (2009) A. S. Hemerly et al. SCIENCE
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- (2008) N. Spassky et al. DEVELOPMENTAL BIOLOGY
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